N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate

Base Information

Chemical Name:N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate
CAS No.:1100768-19-1
Molecular Formula:C₂HF₃O₂*C₂₄H₃₀N₆O₃
Molecular Weight:564.565
Hs Code.:

Synonyms:N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate

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Chemical Property of N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate

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Technology Process of N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate

There total 8 articles about N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 29.0%

: 1100768-22-6
4-(4-{1-[2-(4-carbamimidoyl-phenylcarbamoyl)-acetylamino]-ethyl}-phenyl-carbamoyl)-piperidine-1-carboxylic acid tert-butyl ester trifluoroacetate

: 1100768-19-1
N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate

Guidance literature:: With trifluoroacetic acid; In dichloromethane; at 20 ℃; for 2h;

Reference yield:

: 113117-17-2
ethyl 3-[(4-cyanophenyl)amino]-3-oxopropanoate

: 1100768-19-1
N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate

Guidance literature:: Multi-step reaction with 4 steps

1.1: hydroxylamine hydrochloride; triethylamine / ethanol / 20 h / 20 °C

2.1: ammonium formate / palladium 10% on activated carbon / acetic acid / 5 h / Heating / reflux

2.2: 4 h / 20 °C

3.1: O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 12 h / 20 °C

4.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

With O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate; hydroxylamine hydrochloride; ammonium formate; triethylamine; trifluoroacetic acid; palladium 10% on activated carbon; In ethanol; dichloromethane; acetic acid; N,N-dimethyl-formamide;

Reference yield:

: 1100767-24-5
N-[4-(N-hydroxycarbamimidoyl)-phenyl]-malonamic acid ethyl ester

: 1100768-19-1
N-(4-carbamimidoyl-phenyl)-N'-(1-{4-[(piperidine-4-carbonyl)-amino]-phenyl}-ethyl)-malonamide trifluoroacetate

Guidance literature:: Multi-step reaction with 3 steps

1.1: ammonium formate / palladium 10% on activated carbon / acetic acid / 5 h / Heating / reflux

1.2: 4 h / 20 °C

2.1: O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate / N,N-dimethyl-formamide / 12 h / 20 °C

3.1: trifluoroacetic acid / dichloromethane / 2 h / 20 °C

With O-<[cyano(ethoxycarbonyl)methylene]amino>-1,1,3,3-tetramethyluronium tetrafluoroborate; ammonium formate; trifluoroacetic acid; palladium 10% on activated carbon; In dichloromethane; acetic acid; N,N-dimethyl-formamide;